Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse–Sakati syndrome
Mansoor C. Abdulla Anas M. Alazami Jemshad Alungal Jassim M. Koya Mohthash Musambil
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Mansoor C. Abdulla1 Anas M. Alazami2 Jemshad Alungal1 Jassim M. Koya3 Mohthash Musambil4
Volume 101, 2022
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